ES320727A1 - Phosphorus carbonyl compounds - Google Patents
Phosphorus carbonyl compoundsInfo
- Publication number
- ES320727A1 ES320727A1 ES0320727A ES320727A ES320727A1 ES 320727 A1 ES320727 A1 ES 320727A1 ES 0320727 A ES0320727 A ES 0320727A ES 320727 A ES320727 A ES 320727A ES 320727 A1 ES320727 A1 ES 320727A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- phosphorus
- sulphur
- groups
- oxygen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229910052698 phosphorus Inorganic materials 0.000 title abstract 6
- 239000011574 phosphorus Substances 0.000 title abstract 4
- -1 Phosphorus carbonyl compounds Chemical class 0.000 title abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 5
- 239000005864 Sulphur Chemical group 0.000 abstract 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 5
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 239000001301 oxygen Substances 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 239000012141 concentrate Substances 0.000 abstract 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 230000002363 herbicidal effect Effects 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 230000000361 pesticidal effect Effects 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004437 phosphorous atom Chemical group 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 239000000642 acaricide Substances 0.000 abstract 1
- 150000001266 acyl halides Chemical class 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- 239000003899 bactericide agent Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 238000010410 dusting Methods 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 239000003337 fertilizer Substances 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 150000001455 metallic ions Chemical class 0.000 abstract 1
- 230000001069 nematicidal effect Effects 0.000 abstract 1
- 239000005645 nematicide Substances 0.000 abstract 1
- 239000006072 paste Substances 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 239000004563 wettable powder Substances 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/409—Compounds containing the structure P(=X)-X-acyl, P(=X) -X-heteroatom, P(=X)-X-CN (X = O, S, Se)
- C07F9/4093—Compounds containing the structure P(=X)-X-C(=X)- (X = O, S, Se)
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/095—Compounds containing the structure P(=O)-O-acyl, P(=O)-O-heteroatom, P(=O)-O-CN
- C07F9/096—Compounds containing the structure P(=O)-O-C(=X)- (X = O, S, Se)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1654—Compounds containing the structure P(=X)n-X-acyl, P(=X)n-X-heteroatom, P(=X)n-X-CN (X = O, S, Se; n = 0, 1)
- C07F9/1656—Compounds containing the structure P(=X)n-X-C(=X)- (X = O, S, Se; n = 0, 1)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/307—Acids containing the structure -C(=X)-P(=X)(R)(XH) or NC-P(=X)(R)(XH), (X = O, S, Se)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/32—Esters thereof
- C07F9/3205—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/3247—Esters of acids containing the structure -C(=X)-P(=X)(R)(XH) or NC-P(=X)(R)(XH), (X = O, S, Se)
- C07F9/3252—Esters of acids containing the structure -C(=X)-P(=X)(R)(XH) or NC-P(=X)(R)(XH), (X = O, S, Se) containing the structure -C(=X)-P(=X)(R)(XR), (X = O, S, Se)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/32—Esters thereof
- C07F9/3258—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/3264—Esters with hydroxyalkyl compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4062—Esters of acids containing the structure -C(=X)-P(=X)(XR)2 or NC-P(=X)(XR)2, (X = O, S, Se)
- C07F9/4065—Esters of acids containing the structure -C(=X)-P(=X)(XR)2, (X = O, S, Se)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Novel phosphorus carbonyl compounds of the formula R1R2PX.Y.CO.R3OAr, wherein R1 and R2 each represents an alkyl or aryl group, which may be the same or different and which may be bound to the phosphorus atom through an oxygen atom, X represents oxygen or sulphur, Y represents oxygen or sulphur or a direct phosphorus to carbon bond, R3 represents a linear or branched C1- 3 alkylene radical, and Ar represents a phenyl group which may contain one or more substituents selected from halogen atoms, C1- 4 alkyl groups, C1- 4 alkoxy groups, nitro, -CF3,-CN, formyl and alkoxy-carbonyl groups, are obtained (a) (when Y denotes oxygen or sulphur) by reacting together compounds having the formula R1R2PX.Z and V.CO.R3OAr, wherein one of the groups Z and V denotes the radical -OMe or -SMe and the other is a halogen atom, Me being a metallic or ammonium ion, or (b) (when Y denotes the direct phosphorus-carbon bond) by reacting acyl halides of the formula HalCO.R3.OAr with compounds of the formula R1R2P-R1, wherein R1 is a low-molecular-weight alkoxy or alkylthio group or with compounds of the formula R1R2HPO or R1R2POH. The compounds have pesticidal properties (see Division A5). The phenoxyacyl chlorides used as starting materials may be prepared by reacting the corresponding sodium phenates with chlorocarboxylic and treating the products with thionyl chloride.ALSO:A pesticidal or herbicidal composition contains together with a solid or liquid carrier a compound of the formula R1R2PX.Y.CO.R3 OAr wherein R1 and R2 each represents an alkyl or aryl group, which may be the same or different and which may be bound to the phosphorus atom through an oxygen atom, X represents oxygen or sulphur, Y represents oxygen or sulphur or a direct phosphorus to carbon bond, R3 represents a linear or branched C1-3 alkylene radical and Ar represents a phenyl group which may contain one or more substitutes selected from halogen atoms, C1-4 alkyl groups, C1-4 alkoxy groups, nitro, CF3 CN, formyl and alkoxycarbonyl groups. The carrier may comprise one or more of the following:- a solvent, diluent, dispersing agent, wetting agent, adhesive, fertiliser or other unspecified pesticide, e.g. an insecticide, acaricide, nematocide, bactericide or another fungicide or herbicide. The composition may be in the form of a concentrate, an emulsion concentrate, paste or wettable powder, a sprayable solution or a scattering or dusting agent.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1621264A CH471535A (en) | 1964-12-15 | 1964-12-15 | Pesticides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES320727A1 true ES320727A1 (en) | 1966-05-16 |
Family
ID=4415347
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0320727A Expired ES320727A1 (en) | 1964-12-15 | 1965-12-14 | Phosphorus carbonyl compounds |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3456039A (en) |
| AT (1) | AT258308B (en) |
| BE (1) | BE673589A (en) |
| BR (1) | BR6575681D0 (en) |
| CH (1) | CH471535A (en) |
| DE (1) | DE1518687A1 (en) |
| ES (1) | ES320727A1 (en) |
| FR (1) | FR1487319A (en) |
| GB (1) | GB1113859A (en) |
| IL (1) | IL24755A (en) |
| NL (1) | NL6516265A (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4035176A (en) * | 1975-05-23 | 1977-07-12 | Monsanto Company | N-(perfluoroacyl)-N-phosphonomethyl glycine compounds, method of preparing same |
| EP0007508B1 (en) * | 1978-07-14 | 1983-06-01 | BASF Aktiengesellschaft | Acylphosphinoxide compounds, their preparation and their use |
| US4339443A (en) * | 1978-09-22 | 1982-07-13 | Fbc Limited | Compounds and compositions |
| US4265723A (en) * | 1979-07-06 | 1981-05-05 | Basf Aktiengesellschaft | Photocurable molding, impregnating and coating compositions |
| EP0095115A1 (en) * | 1982-05-26 | 1983-11-30 | Bayer Ag | Substituted diphenyl ethers |
| US5279751A (en) * | 1990-10-01 | 1994-01-18 | Mobil Oil Corporation | Reaction products of sulfur-containing diacyl halides with phosphorodithioic acid and phenols or thiazoles as multifunctional lubricant additives |
| US8859098B2 (en) * | 2012-05-18 | 2014-10-14 | Lord Corporation | Acrylic adhesion promoters |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2719167A (en) * | 1953-04-13 | 1955-09-27 | Ciba Ltd | Compounds containing phosphorus and process therefor |
| US2956919A (en) * | 1955-05-23 | 1960-10-18 | Monsanto Chemicals | 1-oxo-2-halo phosphonates |
| US3009940A (en) * | 1959-12-10 | 1961-11-21 | Stauffer Chemical Co | Dialkylcarbamyl phosphorodithioates as compositions of matter and as pesticides |
| DE1132118B (en) * | 1961-02-01 | 1962-06-28 | Bayer Ag | Process for the preparation of bis (chloromethyl) carbamic acid chloride |
| US3382060A (en) * | 1964-11-18 | 1968-05-07 | Chemagro Corp | Dialkyl and diphenyl esters of aryloxyacetyl-phosphonic acid as herbicides |
-
1964
- 1964-12-15 CH CH1621264A patent/CH471535A/en not_active IP Right Cessation
-
1965
- 1965-12-07 US US512231A patent/US3456039A/en not_active Expired - Lifetime
- 1965-12-08 FR FR41426A patent/FR1487319A/en not_active Expired
- 1965-12-08 IL IL24755A patent/IL24755A/en unknown
- 1965-12-08 GB GB52065/65A patent/GB1113859A/en not_active Expired
- 1965-12-09 DE DE19651518687 patent/DE1518687A1/en active Pending
- 1965-12-10 BE BE673589A patent/BE673589A/xx unknown
- 1965-12-14 AT AT1123665A patent/AT258308B/en active
- 1965-12-14 ES ES0320727A patent/ES320727A1/en not_active Expired
- 1965-12-14 NL NL6516265A patent/NL6516265A/xx unknown
- 1965-12-15 BR BR175681/65A patent/BR6575681D0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE1518687A1 (en) | 1969-02-13 |
| NL6516265A (en) | 1966-06-16 |
| US3456039A (en) | 1969-07-15 |
| IL24755A (en) | 1969-11-30 |
| FR1487319A (en) | 1967-07-07 |
| GB1113859A (en) | 1968-05-15 |
| BR6575681D0 (en) | 1973-11-29 |
| AT258308B (en) | 1967-11-27 |
| CH471535A (en) | 1969-04-30 |
| BE673589A (en) | 1966-06-10 |
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